{3-[4-(4-butyryl-5-methyl-pyrazol-1-yl)phenylcarbamoyl]-5,6-dimethyl-indol-1-yl}acetic acid

Base Information

Chemical Name:{3-[4-(4-butyryl-5-methyl-pyrazol-1-yl)phenylcarbamoyl]-5,6-dimethyl-indol-1-yl}acetic acid
CAS No.:1404529-46-9
Molecular Formula:C₂₇H₂₈N₄O₄
Molecular Weight:472.544
Hs Code.:

Synonyms:{3-[4-(4-butyryl-5-methyl-pyrazol-1-yl)phenylcarbamoyl]-5,6-dimethyl-indol-1-yl}acetic acid

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Chemical Property of {3-[4-(4-butyryl-5-methyl-pyrazol-1-yl)phenylcarbamoyl]-5,6-dimethyl-indol-1-yl}acetic acid

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Technology Process of {3-[4-(4-butyryl-5-methyl-pyrazol-1-yl)phenylcarbamoyl]-5,6-dimethyl-indol-1-yl}acetic acid

There total 24 articles about {3-[4-(4-butyryl-5-methyl-pyrazol-1-yl)phenylcarbamoyl]-5,6-dimethyl-indol-1-yl}acetic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

: 1404532-72-4
{3-[4-(4-butyryl-5-methyl-pyrazol-1-yl)phenylcarbamoyl]-5,6-dimethyl-indol-1-yl}acetic acid methyl ester

: 1404529-46-9
{3-[4-(4-butyryl-5-methyl-pyrazol-1-yl)phenylcarbamoyl]-5,6-dimethyl-indol-1-yl}acetic acid

Guidance literature:: With water; sodium hydroxide; In methanol; at 20 ℃;
DOI:10.1021/jm500588w

Reference yield:

: 99-51-4,34527-23-6,156617-88-8
4-nitro-o-xylene

: 1404529-46-9
{3-[4-(4-butyryl-5-methyl-pyrazol-1-yl)phenylcarbamoyl]-5,6-dimethyl-indol-1-yl}acetic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: palladium 10% on activated carbon; hydrazine hydrate / cyclohexane / 1 h / 0 - 10 °C / Inert atmosphere

1.2: 2 h / 10 °C

2.1: potassium carbonate; methanol / 20 °C

3.1: dmap; sodium hydroxide / tetrahydrofuran / 3 h / 0 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

5.1: palladium 10% on activated carbon; ammonium formate / methanol / 12 h / Inert atmosphere; Reflux

6.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / 1,2-dichloro-ethane / 20 °C

7.1: sodium hydroxide; water / methanol / 20 °C

With methanol; dmap; palladium 10% on activated carbon; water; ammonium formate; potassium carbonate; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; methanol; cyclohexane; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1021/jm500588w

Reference yield:

: 1404532-13-3
1-methoxycarbonylmethyl-5,6-dimethyl-1H-indole-3-carboxylic acid

: 1404529-46-9
{3-[4-(4-butyryl-5-methyl-pyrazol-1-yl)phenylcarbamoyl]-5,6-dimethyl-indol-1-yl}acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / 1,2-dichloro-ethane / 20 °C

2: sodium hydroxide; water / methanol / 20 °C

With dmap; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In methanol; 1,2-dichloro-ethane;
DOI:10.1021/jm500588w